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Vitamin D status and bone density in steroid-treated children with glomerulopathies: effect of cholecalciferol and calcium supplementation

Advances in medical sciences, 2012-06, Vol.57 (1), p.88-93

2012

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Retrospective cohort study of familial hypomagnesaemia with hypercalciuria and nephrocalcinosis due to CLDN16 mutations

Nephrology, dialysis, transplantation, 2015-04, Vol.30 (4), p.636-644

2015

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Intracellular cytokines of peripheral blood lymphocytes in nephrotic syndrome

Pediatric nephrology (Berlin, West), 2002-09, Vol.17 (9), p.733-740

2002

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Rationale, design and objectives of ARegPKD, a European ARPKD registry study

BMC nephrology, 2015-02, Vol.16 (1), p.22-22, Article 22

2015

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Beneficial in vitro effect of N-acetyl-cysteine on oxidative stress and apoptosis

Pediatric nephrology (Berlin, West), 2005-06, Vol.20 (6), p.725-731

2005

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Apoptosis and antioxidant defense in the nephrotic syndrome

Pediatric nephrology (Berlin, West), 2003-11, Vol.18 (11), p.1116-1121

2003

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Th1/Th2 balance and CD45-positive T cell subsets in primary nephrotic syndrome

Pediatric nephrology (Berlin, West), 2000-08, Vol.14 (8-9), p.779-785

2000

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Abnormal Cytokine Synthesis as a Consequence of Increased Intracellular Oxidative Stress in Children Treated with Dialysis

Nephron. Clinical practice, 2005-01, Vol.101 (2), p.c100-c108

2005

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Increased apoptosis of peripheral blood lymphocytes in children with nephrotic syndrome

Pediatric nephrology (Berlin, West), 2002-03, Vol.17 (3), p.197-200

2002

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Dietary antioxidants and total antioxidant status in children with nephrotic syndrome

Polski merkuriusz lekarski, 2001-04, Vol.10 (58), p.237

2001

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Resistance to therapy in primary nephrotic syndrome: effect of MDR1 gene activity

Polski merkuriusz lekarski, 2000-04, Vol.8 (46), p.218

2000

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The copy number variation landscape of congenital anomalies of the kidney and urinary tract

Nature genetics, 2019-01, Vol.51 (1), p.117-127

2019

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Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study

Annals of internal medicine, 2018-01, Vol.168 (2), p.100

2018

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Detection of X-Linked Variations in SHROOM4 in Four Families With Syndromic Congenital Anomalies of the Kidney and Urinary Tract (CAKUT): SA-PO572

Journal of the American Society of Nephrology, 2022-11, Vol.33 (11S), p.762-762

2022

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Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy

Nature genetics, 2023-07, Vol.55 (7), p.1091-1105

2023

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Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

The New England journal of medicine, 2017-02, Vol.376 (8), p.742-754

2017

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Treatment and long-term outcome in primary distal renal tubular acidosis

Nephrology, dialysis, transplantation, 2019-06, Vol.34 (6), p.981-991

2019

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Low levels of urinary epidermal growth factor predict chronic kidney disease progression in children

Kidney international, 2019-07, Vol.96 (1), p.214-221

2019

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X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems

Journal of medical genetics, 2023-06, Vol.60 (6), p.587-596

2023

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Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction

American journal of human genetics, 2019-05, Vol.104 (5), p.994-1006

2019

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Distinct characteristics of multisystem inflammatory syndrome in children in Poland

Scientific reports, 2021-12, Vol.11 (1), p.23562-23562, Article 23562

2021

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Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux

Journal of the American Society of Nephrology, 2021-04, Vol.32 (4), p.805-820

2021

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Vitamin D status and bone density in steroid-treated children with glomerulopathies: effect of cholecalciferol and calcium supplementation

Retrospective cohort study of familial hypomagnesaemia with hypercalciuria and nephrocalcinosis due to CLDN16 mutations

Intracellular cytokines of peripheral blood lymphocytes in nephrotic syndrome

Rationale, design and objectives of ARegPKD, a European ARPKD registry study

Beneficial in vitro effect of N-acetyl-cysteine on oxidative stress and apoptosis

Apoptosis and antioxidant defense in the nephrotic syndrome

Th1/Th2 balance and CD45-positive T cell subsets in primary nephrotic syndrome

Abnormal Cytokine Synthesis as a Consequence of Increased Intracellular Oxidative Stress in Children Treated with Dialysis

Increased apoptosis of peripheral blood lymphocytes in children with nephrotic syndrome

Dietary antioxidants and total antioxidant status in children with nephrotic syndrome

Resistance to therapy in primary nephrotic syndrome: effect of MDR1 gene activity

The copy number variation landscape of congenital anomalies of the kidney and urinary tract

Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study

Detection of X-Linked Variations in SHROOM4 in Four Families With Syndromic Congenital Anomalies of the Kidney and Urinary Tract (CAKUT): SA-PO572

Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy

Diverse ancestry whole-genome sequencing association study identifies TBX5 and PTK7 as susceptibility genes for posterior urethral valves

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

Treatment and long-term outcome in primary distal renal tubular acidosis

Low levels of urinary epidermal growth factor predict chronic kidney disease progression in children

X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems

Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO)

Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction

Distinct characteristics of multisystem inflammatory syndrome in children in Poland

Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux

Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations

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